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2. Mutations in beta-myosin S2 that cause familial hypertrophic cardiomyopathy (FHC) abolish the interaction with the regulatory domain of myosin-binding protein-C. Gruen M; Gautel M J Mol Biol; 1999 Feb; 286(3):933-49. PubMed ID: 10024460 [TBL] [Abstract][Full Text] [Related]
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